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The effects of the selective estrogen receptor modulators, methyl‐piperidino‐pyrazole (MPP), and raloxifene in normal and cancerous endometrial cell lines and in the murine uterus
Author(s) -
Davis Angela M.,
Ellersieck Mark R.,
Grimm Kristie M.,
Rosenfeld Cheryl S.
Publication year - 2006
Publication title -
molecular reproduction and development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.745
H-Index - 105
eISSN - 1098-2795
pISSN - 1040-452X
DOI - 10.1002/mrd.20520
Subject(s) - raloxifene , biology , selective estrogen receptor modulator , estrogen receptor , uterus , pyrazole , estrogen , endometrial cancer , cancer research , receptor , cell culture , pharmacology , cell , estrogen receptor beta , microbiology and biotechnology , medicine , endocrinology , cancer , biochemistry , genetics , chemistry , medicinal chemistry , breast cancer
Since estrogens have vital functions in the uterus but might also contribute to endometrial cancer, we sought to determine the in vitro effects of methyl‐piperidino‐pyrazole (MPP), raloxifene, and β‐estradiol on Ishikawa and RL‐95 endometrial cancer, and ovine luminal endometrial (oLE) cell lines and the in vivo effects of these compounds in the rodent uterus. MPP and raloxifene (1 nM) induced significant apoptosis in the endometrial cancer and oLE cell lines compared to β‐estradiol treated and control cells ( P ≤ 0.0001–0.001). To determine the in vivo uterine effects of these compounds, ovariectomized wild‐type (WT) and estrogen receptor‐β knockout (ERβKO) mice were treated with 25, 50, 100, or 150 µg of each compound. Although raloxifene caused no significant increase in uterine weight, the presumptive ERα antagonist, MPP (25–150 µg) increased uterine weight, and cell proliferation significantly relative to vehicle control in WT and ERβKO mice ( P ≤ 0.001). However, MPP did not increase uterine wet weight as effectively as β‐estradiol ( P ≤ 0.0001), and administration of either 50 µg of MPP or raloxifene effectively reversed the positive effects of 50 and 100 µg β‐estradiol. Unexpectedly, in view of the in vitro studies, MPP and raloxifene treatment of ovariectomized mice did not induce apoptosis of the luminal epithelial cells but rather these compounds induced apoptosis of the underlying uterine stromal cells. These results demonstrate that MPP and raloxifene can exert apparently contrasting in vitro versus in vivo effects, and that they have mixed agonist/antagonist action on murine uterine ERα in vivo. Mol. Reprod. Dev. 1034–1044, 2006. © 2006 Wiley‐Liss, Inc.